Allelopathic Polyketides from an Endolichenic Fungus Myxotrichum SP. by Using OSMAC Strategy

Scientific Reports

Volumn 6, Issue , 2016, Pages

  Yuan, Chao ^a   Guo, Yu Hua ^a   Wang, Hai Ying ^b   Ma, Xiao Jun ^a   Jiang, Tao ^a   Zhao, Jun Ling ^a   Zou, Zhong Mei ^a   Ding, Gang ^a  

^a INSTITUTE OF MEDICINAL PLANT DEVELOPMENT   (China)

^b SHANDONG NORMAL UNIVERSITY   (China)

Author keywords

[No Author keywords available]

Indexed keywords

POLYKETIDE;

ALLELOPATHY; ASCOMYCETES; CHEMICAL STRUCTURE; CHEMISTRY; DRUG EFFECTS; GROWTH, DEVELOPMENT AND AGING; ISOLATION AND PURIFICATION; LICHEN (ORGANISM); METABOLISM; MICROBIOLOGY; NUCLEAR MAGNETIC RESONANCE; PLANT ROOT; X RAY CRYSTALLOGRAPHY;

ALLELOPATHY; ASCOMYCOTA; CRYSTALLOGRAPHY, X-RAY; LICHENS; MOLECULAR STRUCTURE; NUCLEAR MAGNETIC RESONANCE, BIOMOLECULAR; PLANT ROOTS; POLYKETIDES;

EID: 84957546901     PISSN: None     EISSN: 20452322     Source Type: Journal    
DOI: 10.1038/srep19350     Document Type: Article

References (15)

1. Paranagama, P. et al. Heptaketides from corynespora sp. inhabiting the Cavern Beard lichen, Usnea cavernosa: first report of metabolites of an endolichenic fungus (1). J Nat Prod 70, 1700-1705 (2007).
2. Fan, Zhang. et al. A thiopyranchromenone and other chromone derivatives from an endolichenic fungus, Preussia Africana. J Nat Prod 75, 230-237 (2012).
3. Harvey, A. L., Edrada-Ebel, R., Quinn, R. J. The re-emergence of natural products for drug discovery in the genomics era. Nat Rev Drug Discov 14, 111-129 (2015).
4. Grond, S., Papastavrou, I., Zeeck, A. Novel-L-Rhamnopyranosides from a single strain of streptomyces by supplement-induced biosynthetic steps. Eur J Org Chem 19, 3237-3242 (2002).
5. Yuan, C. et al. Austdiol, fulvic acid and citromycetin derivatives from an endolichenic fungus, Myxotrichum sp. Phyto Lett 6, 662-666 (2013).
6. Vleggaar, R., Steyn, P. S., Nagel, D. W. Constitution and absolute configuration of austdiol, the main toxic metabolite from Aspergillus ustus. J Chem Soc, Perkin Trans. I, 45-49 (1974).
7. Pieter S, Steyn & Robert, Vleggaar. The Structure of dihydrodeoxy-8-epi-austdiol and the absolute configuration of the azaphilones. J Chem Soc, Perkin Trans. I, 204-206 (1976).
8. Quang, D. N. et al. Sassafrins A-D, new antimicrobial azaphilones from the fungus Creosphaeria sassafras. Tetrahedron 61, 1743-1748 (2005).
9. Takahashi, M., Koyama, K., Natori, S. Four new azophilones from Chaetomium globosum var. flavor-viridae. Chem Pharm Bull 38, 625-628 (1990).
10. Yoshida, E., Fujimoto, H., Yamazaki, M. Isolation of three new azaphilones, Luteusins C, D, and E, from an Ascomycete, Talaromyces luteus. Chem Pharm Bull 44, 284-287 (1996).
11. Di Bari, L., Pescitelli, G., Pratelli, C., Pini, D., Salvadori, P. Determination of absolute configuration of acyclic 1,2-Diols with Mo2(OAc)4. 1. Snatzke's Method Revisited. J Org Chem 66, 4819-4825 (2001).
12. Gorecki, M. et al. Practical method for the absolute configuration assignment of tert/tert 1, 2-diols using their complexes with Mo2 (OAc)4. J Org Chem 72, 2906-2916 (2007).
13. Willian J, Andrioli. et al. Mycoleptones A? C and Polyketides from the Endophyte Mycoleptodiscus indicus. J Nat Prod 77, 70-78 (2014).
14. Fan, P., Hostettmann, K., Lou, H. Allelochemicals of the invasive neophyte Polygonum cuspidatum Sieb., Zucc.(Polygonaceae). Chemoecology 20, 223-227 (2010).
15. Jiao Y. et al. Metabolites from Penicillium sp., an endophytic fungus from the liverwort Riccardia ultifida (L.) S. Gray. Phyto Lett 6, 14-17 (2013).